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	421.	What hinders congenital ectopia lentis patients' follow-up visits? A qualitative study. [electronic resource] by Lin, Jianqiang Gong, Ni Cao, Qianzhong Zhou, Yijing Cai, Yitingxue Jin, Guangming Young, Charlotte Aimee Yang, Jing Wang, Yiyao Zheng, Danying Producer: 20210215 In: BMJ open vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	422.	Risk factors for postoperative complications in lensectomy-vitrectomy with or without intraocular lens placement in ectopia lentis associated with Marfan syndrome. [electronic resource] by Fan, Fan Luo, Yi Liu, Xin Lu, Yi Zheng, Tianyu Producer: 20141110 In: The British journal of ophthalmology vol. 98 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	423.	Identification of a novel FBN1 mutation in a Chinese family with isolated ectopia lentis. [electronic resource] by Liang, Chen Fan, Wei Wu, Sisi Liu, Yi Producer: 20120426 In: Molecular vision vol. 17 Availability: No items available. Save to lists Add to cart (remove)
	424.	A novel FBN1 mutation in a Chinese family with isolated ectopia lentis. [electronic resource] by Yang, Guoxing Chu, Meifang Zhai, Xinling Zhao, Jialiang Producer: 20120709 In: Molecular vision vol. 18 Availability: No items available. Save to lists Add to cart (remove)
	425.	Ophthalmic findings in a family with early-onset isolated ectopia lentis and the p.Arg62Cys mutation of the fibrillin-1 gene (FBN1). [electronic resource] by Zhao, Jun-Hong Jin, Tian-Bo Liu, Qing-Bo Chen, Chao Hu, Hai-Tao Producer: 20130821 In: Ophthalmic genetics vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	426.	Fibrillin degradation by matrix metalloproteinases: implications for connective tissue remodelling. [electronic resource] by Ashworth, J L Murphy, G Rock, M J Sherratt, M J Shapiro, S D Shuttleworth, C A Kielty, C M Producer: 19990630 In: The Biochemical journal vol. 340 ( Pt 1) Availability: No items available. Save to lists Add to cart (remove)
	427.	Is an iris claw IOL a good option for correcting surgically induced aphakia in children? A review of the literature and illustrative case study. [electronic resource] by Barbara, R Rufai, S R Tan, N Self, J E Producer: 20170324 In: Eye (London, England) vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	428.	Neurologic disorders associated with visual loss in childhood. [electronic resource] by Sher, P K Producer: 19850614 In: Neurologic clinics vol. 3 Availability: No items available. Save to lists Add to cart (remove)
	429.	A novel ADAMTSL4 mutation in autosomal recessive ectopia lentis et pupillae. [electronic resource] by Christensen, Anne E Fiskerstrand, Torunn Knappskog, Per M Boman, Helge Rødahl, Eyvind Producer: 20110113 In: Investigative ophthalmology & visual science vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	430.	Ectopia lentis as the presenting and primary feature in Marfan syndrome. [electronic resource] by Zadeh, Neda Bernstein, Jonathan A Niemi, Anna Kaisa Dugan, Sarah Kwan, Andrea Liang, David Hyland, James C Hoyme, H Eugene Hudgins, Louanne Manning, Melanie A Producer: 20120209 In: American journal of medical genetics. Part A vol. 155A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	431.	Novel mutation in FBN1 causes ectopia lentis and varicose great saphenous vein in one Chinese autosomal dominant family. [electronic resource] by Fu, Qing Liu, Peng Lu, Qingsheng Wang, Feng Wang, Hui Shen, Wei Xu, Fei Liu, Lin Sergeev, Yuri V Sui, Ruifang Producer: 20140930 In: Molecular vision vol. 20 Availability: No items available. Save to lists Add to cart (remove)
	432.	Disruption of murine Adamtsl4 results in zonular fiber detachment from the lens and in retinal pigment epithelium dedifferentiation. [electronic resource] by Collin, Gayle B Hubmacher, Dirk Charette, Jeremy R Hicks, Wanda L Stone, Lisa Yu, Minzhong Naggert, Jürgen K Krebs, Mark P Peachey, Neal S Apte, Suneel S Nishina, Patsy M Producer: 20160825 In: Human molecular genetics vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	433.	Acute aortic dissection (Stanford type B) during pregnancy. [electronic resource] by Katsuragi, S Neki, R Yoshimatsu, J Ikeda, T Morisaki, H Morisaki, T Producer: 20140224 In: Journal of perinatology : official journal of the California Perinatal Association vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	434.	Next-generation sequencing reveals a new mutation in the LTBP2 gene associated with microspherophakia in a Spanish family. [electronic resource] by Alías, Laura Crespi, Jaume González-Quereda, Lidia Téllez, Jesús Martínez, Elisabeth Bernal, Sara Gallano, Ma Pia Producer: 20190225 In: BMC medical genetics vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	435.	Congenital ectopia lentis. A Danish national survey. [electronic resource] by Fuchs, J Rosenberg, T Producer: 19980505 In: Acta ophthalmologica Scandinavica vol. 76 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	436.	[Transsclerally fixated intraocular artificial lenses in children--analysis of long-term postoperative complications]. [electronic resource] by Kanigowska, Krystyna Grałek, Mirosława Karczmarewicz, Beata Producer: 20080401 In: Klinika oczna vol. 109 Availability: No items available. Save to lists Add to cart (remove)
	437.	Glaucoma in children. [electronic resource] by Chew, E Morin, J D Producer: 19840126 In: Pediatric clinics of North America vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	438.	Sensitivity of conformation sensitive gel electrophoresis in detecting mutations in Marfan syndrome and related conditions. [electronic resource] by Körkkö, J Kaitila, I Lönnqvist, L Peltonen, L Ala-Kokko, L Producer: 20020312 In: Journal of medical genetics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	439.	Humphrey visual fields and optical coherence tomography findings in patients with the Axenfeld-Rieger syndrome: a case series. [electronic resource] by Santiago-Cabán, Luis A Colón-Casasnovas, Jaime E Izquierdo, Natalio J Producer: 20110811 In: Boletin de la Asociacion Medica de Puerto Rico vol. 102 Availability: No items available. Save to lists Add to cart (remove)
	440.	ADAMTSL4, a secreted glycoprotein widely distributed in the eye, binds fibrillin-1 microfibrils and accelerates microfibril biogenesis. [electronic resource] by Gabriel, Luis A R Wang, Lauren W Bader, Hannah Ho, Jason C Majors, Alana K Hollyfield, Joe G Traboulsi, Elias I Apte, Suneel S Producer: 20120327 In: Investigative ophthalmology & visual science vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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